Fabrice Odefrey

5.4k total citations
10 papers, 374 citations indexed

About

Fabrice Odefrey is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Fabrice Odefrey has authored 10 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Cancer Research and 3 papers in Molecular Biology. Recurrent topics in Fabrice Odefrey's work include BRCA gene mutations in cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and Genetic factors in colorectal cancer (3 papers). Fabrice Odefrey is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and Genetic factors in colorectal cancer (3 papers). Fabrice Odefrey collaborates with scholars based in Australia, United States and France. Fabrice Odefrey's co-authors include Melissa C. Southey, John L. Hopper, David E. Goldgar, Graham G. Giles, Carmel Apicella, Daniel J. Park, Graham Byrnes, James G. Dowty, Ingrid Winship and Zhi L. Teo and has published in prestigious journals such as Cancer Research, British Journal of Cancer and BMC Bioinformatics.

In The Last Decade

Fabrice Odefrey

10 papers receiving 364 citations

Peers

Countries citing papers authored by Fabrice Odefrey

Since Specialization

Citations

This map shows the geographic impact of Fabrice Odefrey's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fabrice Odefrey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fabrice Odefrey more than expected).

Fields of papers citing papers by Fabrice Odefrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fabrice Odefrey. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fabrice Odefrey. The network helps show where Fabrice Odefrey may publish in the future.

Co-authorship network of co-authors of Fabrice Odefrey

This figure shows the co-authorship network connecting the top 25 collaborators of Fabrice Odefrey. A scholar is included among the top collaborators of Fabrice Odefrey based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fabrice Odefrey. Fabrice Odefrey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets 2013 ·BMC Bioinformatics ·Bernard J. Pope, Tú Nguyen‐Dumont, Fabrice Odefrey, Fleur Hammet, Russell Bell, Kayoko Tao, Sean V. Tavtigian, David E. Goldgar, Andrew Lonie, Melissa C. Southey, Daniel J. Park	6
2	Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families 2013 ·Breast Cancer Research ·Zhi L. Teo, Daniel J. Park, Elena Provenzano, Catherine Chatfield, Fabrice Odefrey, Tú Nguyen‐Dumont, (unknown), James G. Dowty, John L. Hopper, Ingrid Winship, David E. Goldgar, Melissa C. Southey	34
3	Explaining Variance in the Cumulus Mammographic Measures That Predict Breast Cancer Risk: A Twins and Sisters Study 2013 ·Cancer Epidemiology Biomarkers & Prevention ·Tuong L. Nguyen, Daniel F. Schmidt, Enes Makalic, Gillian S. Dite, Jennifer Stone, Carmel Apicella, Minh Bui, Robert J. MacInnis, Fabrice Odefrey, Jennifer Cawson, Susan A. Treloar, Melissa C. Southey, Graham G. Giles, John L. Hopper	31
4	FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer 2011 ·Breast Cancer Research and Treatment ·Daniel J. Park, Fabrice Odefrey, Fleur Hammet, Graham G. Giles, Laura Baglietto, (unknown), (unknown), John L. Hopper, Daniel F. Schmidt, Enes Makalic, Olga M. Sinilnikova, David E. Goldgar, Melissa C. Southey	12
5	A PALB2 mutation associated with high risk of breast cancer 2010 ·Breast Cancer Research ·Melissa C. Southey, Zhi L. Teo, James G. Dowty, Fabrice Odefrey, Daniel J. Park, Marc Tischkowitz, Nelly Sabbaghian, Carmel Apicella, Graham Byrnes, Ingrid Winship, Laura Baglietto, Graham G. Giles, David E. Goldgar, William D. Foulkes, John L. Hopper, (unknown), (unknown)	89
6	Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease 2010 ·Cancer Research ·Fabrice Odefrey, Jennifer Stone, Lyle C. Gurrin, Graham Byrnes, Carmel Apicella, Gillian S. Dite, Jennifer Cawson, Graham G. Giles, Susan A. Treloar, Dallas R. English, John L. Hopper, Melissa C. Southey, (unknown)	61
7	Are *ATM* Mutations 7271T→G and IVS10-6T→G Really High-Risk Breast Cancer-Susceptibility Alleles? 2004 ·Cancer Research ·Csilla I. Szabo, Mieke Schutte, Annegien Broeks, Jeanine J. Houwing‐Duistermaat, Yvonne R. Thorstenson, Francine Durocher, Rogier A. Oldenburg, Marijke Wasielewski, Fabrice Odefrey, Deborah J. Thompson, Arno Floore, Jaco Kraan, Jan G.M. Klijn, Ans M.W. van den Ouweland, (unknown), Teresa Wagner, Peter Devilee, Jacques Simard, Laura van ‘t Veer, David E. Goldgar, Hanne Meijers‐Heijboer	43
8	Germline truncating mutations in both MSH2 and BRCA2 in a single kindred 2004 ·British Journal of Cancer ·Isabelle Thiffault, Nancy Hamel, Tuya Pal, (unknown), Victoria Marcus, Debora B. Farber, Shannon Cowie, Jean Deschênes, Wendy S. Meschino, Fabrice Odefrey, David E. Goldgar, Tracy Graham, Steven A. Narod, Andrea Watters, Elizabeth MacNamara, Desirée du Sart, George Chong, William D. Foulkes	31
9	Haplotype analysis of theBRCA29254delATCAT recurrent mutation in breast/ovarian cancer families from Spain 2003 ·Human Mutation ·Berta Campos, Orland Dı́ez, Fabrice Odefrey, Montserrat Domènech, Virginie Moncoutier, José I. Martínez‐Ferrandis, Ana Osório, Judith Balmañà, Alicia Barroso, M.‐Eugenia Armengod, Javier Benı́tez, Carmen Alonso, Dominique Stoppa‐Lyonnet, David E. Goldgar, Montserrat Baiget	18
10	BRCA1andBRCA2mutation analysis of early-onset and familial breast cancer cases in Mexico 2002 ·Human Mutation ·Pablo Ruíz-Flores, Olga M. Sinilnikova, Michael D. Badzioch, Ana Laura Calderón‐Garcidueñas, (unknown), Fabrice Odefrey, Juan Francisco González-Guerrero, Csilla I. Szabo, Gilbert Lenoir, David E. Goldgar, Hugo A. Barrera‐Saldaña	49

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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